mivazerol
Sign in to saveMivazerol is an α2-adrenergic receptor agonist.
Research
35 papers- Mivazerol, a novel alpha2-agonist and potential anti-ischemic drug, inhibits KC1-stimulated neurotransmitter release in rat nervous tissue preparations.Journal of neurochemistry · 1996
- Mivazerol, a new alpha 2-adrenergic agonist, blunts cardiovascular effects following surgical stress in pentobarbital-anesthetized rats.Acta anaesthesiologica Scandinavica · 1997
- Effect of mivazerol on perioperative cardiac complications during non-cardiac surgery in patients with coronary heart disease: the European Mivazerol Trial (EMIT).Anesthesiology · 1999
- Mivazerol inhibits intrathecal release of glutamate evoked by halothane withdrawal in rats.Acta anaesthesiologica Scandinavica · 1998
- Mivazerol, a novel compound with high specificity for alpha 2 adrenergic receptors: binding studies on different human and rat membrane preparations.Neurochemistry international · 1994
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 217.085
Show 3 more facts
- chemical formula
- C₁₁H₁₁N₃O₂
- canonical SMILES
- C1=CC(=C(C(=C1)CC2=CN=CN2)O)C(=O)N
- subject has role
- alpha-adrenergic agonist
Sources (2)
via Wikidata · CC0
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Encyclopedic overview
1 sectionsContents
- References
Mivazerol is an α2-adrenergic receptor agonist.
==References==
Excerpted from Wikipedia’s “mivazerol” article, available under the CC BY-SA 4.0 licence.